NDC 43547-361 – Losartan Potassium

Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC43547-361

Product details

Brand name
Losartan Potassium
Generic name
Losartan potassium
Labeler
Solco Healthcare US, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091497
Marketed since
March 20, 2022
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losartan potassium →

Package NDC codes (4)

Package NDCDescriptionSince
43547-361-0330 TABLET, FILM COATED in 1 BOTTLE (43547-361-03)Mar 20, 2022
43547-361-0990 TABLET, FILM COATED in 1 BOTTLE (43547-361-09)Mar 20, 2022
43547-361-111000 TABLET, FILM COATED in 1 BOTTLE (43547-361-11)Mar 20, 2022
43547-361-50500 TABLET, FILM COATED in 1 BOTTLE (43547-361-50)Mar 20, 2022

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